- FUJIFILM Holdings America Corporation (Boston, MA)
- Overview The Associate Director / Director of Business Development, will be an ambitious salesperson who independently works to identify, qualify, negotiate, ... calls with C-level and senior leaders at client accounts; prepare and lead presentations and facilitate site visitsWork closely and collaboratively with Project… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …well as other research areas centered around rare diseases and immune disorders. **Summary** CMC Lead is responsible for supporting the overall CMC ... based on the project needs and the respective development stage of the project. The CMC Lead will support the Sr. CMC Lead on complex and/or late-stage… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …The Technology Management (mAb, Drug Substance, Drug Product, or New Modality) Lead is responsible for the management of technology transfer of the manufacturing ... (mAb, Drug Substance, Drug Product, or New Modality) manufacturing, evaluates CMC risks for appropriate escalation, recommends transition milestones and ensures a… more
- Sumitomo Pharma (Columbus, OH)
- …and management of the global contract testing laboratories in partnership with the Company's CMC Team. The Associate Director also participates in drafting ... ** Associate Director , GMP Quality Control** Sumitomo...analyses, reports, and recommend product expiry extensions/reductions, as applicable. Lead and/or present at the Stability and Specification Review… more
- CSL Behring (King Of Prussia, PA)
- …biotherapies used to treat serious and often rare conditions. Could you be our next Associate Director , R&D Master Scheduling Lead ? This position is located ... in our King of Prussia PA office. It is a Hybrid role. The Associate Director , R&D Project Planning Capability Lead , is a member of CSL R&D's Project and… more
- Teva Pharmaceuticals (West Chester, PA)
- Associate Director , Regulatory Affairs - West Chester, PA Date: Apr 24, 2024 Location: West Chester, United States, 1938 Company: Teva Pharmaceuticals Job Id: ... difference with. **How you'll spend your day** As the Associate Director , Regulatory Affairs you will be...responsible for acting as and supporting the Global Regulatory Lead (GRL) in strategic vision and innovative scientific and… more
- Sanofi Group (Framingham, MA)
- …Culture Development department within CCD located in Framingham, MA in the role of Associate Director . We are looking for a candidate with excellent scientific, ... CMC , communication, and management skills to manage a team of upstream scientists and lead cross-functional projects. As a senior staff member of Commercial Cell… more
- Novo Nordisk (Watertown, MA)
- …Development - Boston and will work closely with other functions of CMC drug development, including Drug Product, Analytical Sciences, Quality Assurance, and Supply ... larger Chemical Development organization anchored in Denmark. Essential Functions + Lead and manage external API development and manufacturing activities +… more
- Boehringer Ingelheim (North Brunswick, NJ)
- …Ingelheim has a career opportunity developing pharmaceutical products as a Senior Associate Director , Analytical Development. We are looking for an individual ... in development. You will represent the Analytical Development function in the CMC -Technical Development Team whenever needed and pro-actively help the team to… more
- Sanofi Group (Bridgewater, NJ)
- …Global Regulatory Team (GRT), and strategic partner to the Global Regulatory Lead (GRL), the Regulatory Specialist leverages their regulatory expertise to contribute ... business planning, governance, and committees. May be requested to lead Global Regulatory Team meetings + May represent GRT...strategy in collaboration with non-US - non-EU regions / GRA- CMC / GRA-Devices. Attends HA meetings and collaborates with… more
- Gilead Sciences, Inc. (Foster City, CA)
- …than 35 countries worldwide, with headquarters in Foster City, California. ** Associate Director , Strategic Sourcing and Supplier Management, Primary Packaging ... leaders to step up, share ideas, listen, learn, and lead . We're welcoming bright, diverse, and imaginative minds; we're...Components** **KEY RESPONSIBILITIES** The Associate Director , Strategic Sourcing & Supplier Management,… more
- Sanofi Group (Bridgewater, NJ)
- …Global Regulatory Team (GRT), and strategic partner to the Global Regulatory Lead (GRL), the Regulatory Strategist leverages their regulatory expertise to contribute ... business planning, governance, and committees. May be requested to lead Global Regulatory Team meetings + May represent GRT...strategy in collaboration with non-US - non-EU regions / GRA- CMC / GRA-Devices. Attends HA meetings and collaborates with… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …on real-world evidence, and creating hope for all facing illness. The Associate Director , Business Development will seek out potential business opportunities ... efficiently communicating with excellent facilitation. The incumbent will also lead initial partnership, licensing and/or acquisition negotiations with sufficient… more
- Bristol Myers Squibb (Summit, NJ)
- …their personal lives. Read more: careers.bms.com/working-with-us . Position Summary: The Associate Director Supplier Relationship Manager (SRM) is accountable ... BMS vision. The SRM acts as a manufacturing site lead and is accountable for the performance of the...alignment of objectives and priorities with GO Teams and CMC teams, representing the virtual matrix team and CMOs… more
- Merck (Rahway, NJ)
- …culture, talent development, technology introduction, and compliance. However, one co- lead remains focused on non-sterile pipeline programs and infrastructure while ... one co- lead remains focused on sterile pipeline programs and infrastructure....is based in New Jersey and reports to the Associate Vice President of Pharmaceutical Operations and Clinical Supply… more
- Merck (Boston, MA)
- …to customers both internal and external to GCS and serves as the lead GCS spokesperson at clinical and development related meetings. Working independently, the ... limited to:** + Interacts closely with key partner organizations (as a lead GCS Planning program representative) such as clinical development, regulatory, quality… more
- AbbVie (North Chicago, IL)
- …Clinical Pharmacology and Pharmacometrics management. Responsibilities: + Executes strategy, lead teams and various data analyses and interpretation by providing ... groups to provide a unified modeling and simulation position to clinical, CMC and regulatory teams. + Responsible for the appropriateness, quality and accuracy… more
- Merck (Rahway, NJ)
- …for a range of modalities including small molecules and peptides. Within OFS, the Director will influence the strategy, lead activities, and develop a team whose ... organizations (Research Division/Manufacturing Division), such as Analytical, Quality, Regulatory CMC , and technical functions, to ensure timebound progression of… more
- AbbVie (Madison, NJ)
- …with multiple driver indications within a Therapeutic Area and support the Manager, Global Regulatory Lead (GRL), Associate Director , or Director , in the ... timely response to Health Authorities during application review. . Support CMC sections of major, complex regulatory submissions, including Investigation New Drugs… more
- UTMB Health (Dallas, TX)
- …Department (TJJD). **_JOB SUMMARY_** **:** Works under the direction of the Associate Medical Director . **_ESSENTIAL JOB FUNCTIONS (Medical Director )_** ... and recommends institutional policies and procedures that will enable UTMB CMC to maximize Digital Medical Services/Telemedicine. + Contributes to the development… more
